Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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MRI Tubing Kit Extension:The Selector tubing connects the handpiece to the IV fluid and connects the handpiece to the suction canister on the CUSA® Selector / CUSA NXT console.
INTEGRA LIFESCIENCES (IRELAND) LIMITED
1532024
Not in Commercial Distribution

  • 30381780040259 ()
  • 10381780040255 ()
  • M26915320241 ()


  • Surgical irrigation/aspiration tubing set
Microsurgical - Box Of 10: The Selector tubing connects the handpiece to the IV fluid and connects the handpiece to the suction canister on the CUSA® Selector / CUSA NXT console.
INTEGRA LIFESCIENCES (IRELAND) LIMITED
1529036
Not in Commercial Distribution

  • 30381780040242 ()
  • 10381780040248 ()
  • M26915290361 ()


  • Soft-tissue ultrasonic surgical system handpiece tip, single-use
3M™ Curos™ Jet™ Disinfecting Cap for Needleless Connectors 270/Carton 20 Cartons/Case CFJ1-270
3M COMPANY
CFJ1-270
In Commercial Distribution

  • 50707387773828 ()
  • 30707387773824 ()
  • 00707387773823 ()
CFJ1-270

  • Luer-formatted disinfection cap
No Description
Bionova Medical Inc.
500-1020
In Commercial Distribution

  • 00850047730299 ()

  • Length: 10 Centimeter
  • Width: 20 Centimeter


  • Cavity-wound management dressing, non-antimicrobial
Perforated
Bionova Medical Inc.
902-2025
In Commercial Distribution

  • 00850047730183 ()

  • Length: 20 Centimeter
  • Width: 25 Centimeter


  • Wound regenerating polysaccharide agent
No Description
Bionova Medical Inc.
802-2025
In Commercial Distribution

  • 00850047730145 ()

  • Length: 20 Centimeter
  • Width: 25 Centimeter


  • Wound regenerating polysaccharide agent
No Description
Bionova Medical Inc.
501-1020
In Commercial Distribution

  • 00850047730107 ()

  • Length: 10 Centimeter
  • Width: 20 Centimeter


  • Cavity-wound management dressing, non-antimicrobial
Fish-Skin Graft for Surgical Use. Kerecis® SurgiClose® is indicated for the management of wounds including: Partial and full thickness wounds, pressure ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor site/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds. IFU: https://www.kerecis.com/ifus/ifu-kerecis-surgiclose/
KERECIS hf.
7x20 cm Meshed 2:1
In Commercial Distribution

  • 05694310961165 ()
  • 05694310961158 ()

  • Length: 7 Centimeter
  • Width: 20 Centimeter
50205N21D0D

  • Animal-derived wound matrix dressing
Acellular fish skin for topical and surgical wounds. INTENDED USE Kerecis® Burn is indicated for the management of wounds including: - Partial and full-thickness wounds, - Trauma wounds (abrasions, lacerations, second-degree burns, skin tears). Mesh ratio 2:1 Double Pouched https://www.kerecis.com/wp-content/uploads/2020/10/A5-KM-19-0146-IFU-Kerecis-Burn-US.pdf
KERECIS hf.
7x20 Meshed Burn
In Commercial Distribution

  • 05694310961127 ()
  • 05694310961110 ()

  • Length: 7 Centimeter
  • Width: 20 Centimeter
50202N21D0D

  • Animal-derived wound matrix dressing
Fish-Skin Graft for Surgical Use. Kerecis® SurgiClose® is indicated for the management of wounds including: Partial and full thickness wounds, pressure ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor site/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds. IFU: https://www.kerecis.com/ifus/ifu-kerecis-surgiclose/
KERECIS hf.
7x20 cm
In Commercial Distribution

  • 05694310960724 ()
  • 05694310960731 ()

  • Length: 7 Centimeter
  • Width: 20 Centimeter
50205S21D0D

  • Animal-derived wound matrix dressing
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